A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17629581



Internal ID21821628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67731240..67731518hg38UCSC Ensembl
chr17:65727356..65727634hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6037868
Supporting Variants
Samples
Known GenesNOL11
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17629581
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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